Nonthermal plasma-promoted CO2 hydrogenation in presence of alloy catalysts

Climate change accelerated by excess CO₂ emissions has been a major concern over the past few years. To deal with this problem, technologies that can not only reduce and remove excess CO₂ emissions but also transform them into value-added chemicals are being developed. One such method is the hydrogenation of CO₂ using renewable hydrogen to produce alternative fuels.

Over the years different strategies have been developed to improve CO₂ hydrogenation in the presence of metallic catalysts. The most promising among them is nonthermal plasma (NTP). It promotes hydrogenation of CO₂ beyond the thermodynamic limit even at low temperatures without deactivating metallic catalysts, which are vulnerable to higher temperatures. Despite the rising popularity of this technique, the interactions between the NTP-activated species and metallic catalysts are still not well understood.

Fortunately, a team of researchers from Tokyo Institute of Technology (Tokyo Tech), Japan, led by Prof. Tomohiro Nozaki, devised a study to overcome this gap in understanding. In their recent breakthrough, published in the Journal of the American Chemical Society, the researchers revealed the reaction dynamics for NTP-assisted CO₂ hydrogenation on the surface of Pd₂Ga/SiO₂ alloy catalysts that lead to the formation of formate. Prof Nozaki explains "Reaction mechanisms like Eley-Rideal or E-R pathway have been proposed to explain efficient CO₂ conversion at lower temperatures and the activation energy for this reaction decreases dramatically. Moreover, NTP produces a copious amount of vibrationally activated CO₂ which is the key to enhancing CO₂ conversion beyond the thermal equilibrium."

The team investigated the reactions between NTP activated CO₂ and Pd₂Ga/SiO₂ alloy catalysts in a fluidized-bed dielectric barrier discharge reactor  and compared them to conventional thermal catalysis. The results revealed that the CO₂ conversion into formate was more than two-fold in the case of NTP-assisted hydrogenation when compared to thermal conversion. To further establish the mechanics of the mentioned conversion, the scientists adopted in situ spectroscopic analysis and density functional theory (DFT) calculations.

The results revealed that the NTP activation gave rise to vibrationally excited CO₂ molecules which directly react with hydrogen atoms adsorbed by the Pd sites on the catalyst via the E-R pathway. One of the O atoms from the reacted species then got adsorbed at the neighboring Ga site resulting in the formation of monodentate-formate or m-HCOO. The DFT calculations also deduced a decomposition pathway for the same m-HCOO species.

This experimental-theoretical study showed that NTP can promote CO₂ hydrogenation to limits those conventional thermal methods can hardly reach. It also provided mechanistic insights into NTP activated CO₂ and catalyst interaction, which can be utilized to develop better catalysts and improve the hydrogenation process. "With our research, we wanted to accelerate the waste to wealth initiative. Capturing CO₂ and using it as feedstock for synthesis of fuels and valuable chemicals will not only help us deal with climate problem but also slow down fossil fuel depletion to some extent," concludes Prof. Nozaki.